Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/114913
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dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.contributorResearch Institute for Smart Energy-
dc.creatorQin, Y-
dc.creatorZhang, C-
dc.creatorWang, Y-
dc.creatorShe, P-
dc.creatorWong, WY-
dc.date.accessioned2025-09-01T01:53:45Z-
dc.date.available2025-09-01T01:53:45Z-
dc.identifier.urihttp://hdl.handle.net/10397/114913-
dc.language.isoenen_US
dc.publisherJohn Wiley & Sons, Inc.en_US
dc.rightsThis is an open access article under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits use, distribution and reproduction in any medium, provided the original work is properly cited.en_US
dc.rights© 2025 The Author(s). Carbon Energy published by Wenzhou University and John Wiley & Sons Australia, Ltd.en_US
dc.rightsThe following pubication Qin, Y., Zhang, C., Wang, Y., She, P. and Wong, W.-Y. (2025), Electrostatic Attraction-Driven Assembly of Non-Noble Metallo-Supramolecular Polymers With Single-Walled Carbon Nanotubes for Boosting Photocatalytic Hydrogen Evolution. Carbon Energy, 7: e70003 is available at https://doi.org/10.1002/cey2.70003.en_US
dc.subjectElectrostatic attractionen_US
dc.subjectHybrid heterojunctionen_US
dc.subjectMetallo‐supramolecular polymersen_US
dc.subjectPhotocatalytic hydrogen evolutionen_US
dc.subjectSingle‐walled carbonnanotubesen_US
dc.titleElectrostatic attraction-driven assembly of non-noble metallo-supramolecular polymers with single-walled carbon nanotubes for boosting photocatalytic hydrogen evolutionen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume7-
dc.identifier.issue6-
dc.identifier.doi10.1002/cey2.70003-
dcterms.abstractThe search for photoactive materials that are able to efficiently produce solar fuels is a growing research field to tackle the current energy crisis. Herein, we have prepared two ionic non-noble metallo-supramolecular polymers Se-MTpy (M = Co or Ni), and constructed their composites with single-walled carbon nanotubes (CNTs) via electrostatic attraction and π–π interactions for efficient and stable photocatalytic hydrogen evolution. In the photocatalytic system, the cationic Se-MTpy as host and anionic CNTs as guest are assembled into a binary composite, which exhibits superior photocatalytic activity under visible light irradiation (> 420 nm). The optimized CNT@Se-CoTpy composite, containing 1.2 wt% metal loading, achieves 7 times higher hydrogen evolution rate (2.47 mmol g−1 h−1) than bare Se-CoTpy (0.35 mmol g−1 h−1). This is attributed to the constructive formation of junctions between polymer and CNTs, facilitating interfacial charge transfer and transport for efficient proton reduction. The composite system also shows high photostability after continuous irradiation for ~30 h. The combination of experimental and theoretical analysis demonstrates the higher activity for reducing H2O to H2 of Se-CoTpy than Se-NiTpy. The feasible interfacial architecture proposed in this study represents an effective approach to achieve high photocatalytic performance.-
dcterms.abstractGraphical abstract: [Figure not available: see fulltext.]-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationCarbon energy, June 2025, v. 7, no. 6, e70003-
dcterms.isPartOfCarbon energy-
dcterms.issued2025-06-
dc.identifier.eissn2637-9368-
dc.identifier.artne70003-
dc.description.validate202509 bcch-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_TAen_US
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThis work was financially supported by the RGC Senior Research Fellowship Scheme (SRFS2021-5S01), the Hong Kong Research Grants Council (PolyU 15307321), Research Institute for Smart Energy (CDAQ), Research Centre for Nanoscience and Nanotechnology (CE2H), Research Centre for Carbon-Strategic Catalysis (CE2L), Miss Clarea Au for the Endowed Professorship in Energy (847S), and National Natural Science Foundation of China (62205277).en_US
dc.description.pubStatusPublisheden_US
dc.description.TAWiley (2025)en_US
dc.description.oaCategoryTAen_US
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